Oishi Shinya | Laboratory Of Medicinal Chemistry Ccr Nci Nih

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著作論文

Synthesis of a CC Chemokine, vMIP-II, Encoded by Kaposi's Sarcoma-Associated Herpesvirus and Its Biological Activity
Development of the Chemokine Receptor CXCR4 Antagonists as Multi-Pharmaceutical Agents Involving a New Class of Low Molecular Weight Antagonists
P-423 Structure-Activity Relationship Studies on Cyclic Peptide-Based CXCR4 Antagonists
Synthesis and Biological Evaluation of Peptidomimetic Analogs of the CXCR4 Antagonist FC131
A New Strategy for Molecular-size Reduction of Bioactive Peptide, Using Two Orthogonal Libraries of Cyclic peptides
Development of Specific CXCR4 Inhibitors Based on an Anti-HIV Peptide, T140, and Their Structure-Activity Relationships Study
Helix Inducible Motifs Affect Helicity and Bioactivity of Anti-HIV Peptides
Application of β-Branched Allylglycine Equivalents to Macrocyclic Grb2 SH2 Domain-Binding Inhibitors
Efficient Synthesis of Cyclic RGD Pseudopeptide with (E)-Alkene Dipeptide Isostere and Its Biological Activity
Synthesis and Application of Novel Fluorescence-Labeled CXCR4 Antagonists
P-467 Structure-activity relationship study on GPR54 agonists
Structure-Activity Relationship Study on hOT7T175 Agonist with RW-Amide
Endeavors for Highly Stereoselective Synthesis of Functionalized Fluoroalkene Dipeptide Isosteres
Synthesis of ψ[(E)-CH=CMe]- and ψ[(Z)-CH=CMe]-type Dipeptide Isosteres and their Application to a Cyclic RGD Peptide
Synthesis of ψ[(E)-CMe=CMe]- and ψ[(E)-CMe=CH]-type Alkene Dipeptide Isosteres from a Chiral Amino Acid
Properties of Intracellular Fragment Peptides of Mouse Prostaglandin E_2 Receptor EP3 Isoform
Inhibitory Effect of Newly Developed CXC-Chemokine Receptor 4 Antagonists on the Infection with Feline Immunodeficiency Virus(Virology)
Specific Fluorescence Labeling of Membrane Receptors in Living Cells using Coiled-coil Tag
Fluoroalkene Skeleton as a Peptide Bond Mimetic : Its Scope and Limitations
Establishment and Clinical Application of an Enzyme Immunoassay for Metastin to Determination of the Human Plasma Levels
A Novel Oxazolidine Linker for the Synthesis of Peptide Aldehydes
Structure-Activity Relationship Studies on GPR54 Agonists
Development of Low Molecular Weight CXCR4 Antagonists by Exploratory Structural Tuning of Cyclic Tetrapeptide-scaffolds
Cyclic Analogs Derived from Laminin Enhanced the Biological Activities
Biological Activity of a Cyclic Peptide from Laminin α1 Chain Loop Region
Synthesis and Application of Novel Phosphotyrosyl Mimetics to Grb2 SH2 Domain-Binding Inhibitors
Application of Ring Closing Olefin Metathesis to the Conformational Restriction of Biologically Active Peptide. Part 1
Identification of Novel HIV-1 Fusion Inhibitors by Template-Assisted Peptide Aldehyde Ligation
Structure Activity Relationship Study of the Helix-inducible Motifs in HIV Fusion Inhibitors
X-ray Crystallographic Study of the HIV-1 Fusion Inhibitor against the Drug-Resistant N43D Variant
Bioorganic Synthesis of End-capped HIV-1 Fusion Inhibitor SC35EK
Development of Novel GPR54 Agonists with Resistance to Degradation by MMP
Diastereoselective Synthesis of (Z)-Fluoroalkene Dipeptide Isostere and the Application to a HIV Membrane Fusion Inhibitor
Diastereoselective Synthesis of Trifluoromethylalkene Dipeptide Isosteres Based on Nucleophilic Trifluoromethylation
New Strategy for The Synthesis of Aspartyl Protease Inhibitor Based on "Aza-Payne Rearrangement"
Utility of Plasma Bioactive Peptides Levels as Biomarkers
Stereoselective Synthesis of Tyr-Orn Type Alkene Dipeptide Isosteres and Their Application to Bioactive Peptides
Functional Characterization of Kisspeptin Receptor Ligands : Activation of Neuropeptide FF Receptors
Synthetic Studies on Coibamide A

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